Discovery of 2208-59-5

This literature about this compound(2208-59-5)Related Products of 2208-59-5has given us a lot of inspiration, and I hope that the research on this compound(2-(Pyridin-4-yl)-1H-benzo[d]imidazole) can be further advanced. Maybe we can get more compounds in a similar way.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 2-(Pyridin-4-yl)-1H-benzo[d]imidazole(SMILESS: C1(C2=CC=NC=C2)=NC3=CC=CC=C3N1,cas:2208-59-5) is researched.Recommanded Product: 2-Chloropyridine 1-oxide. The article 《Effects of 2-arylbenzimidazoles on rat hepatic microsomal monooxygenase system》 in relation to this compound, is published in Comparative Biochemistry and Physiology, Part C: Pharmacology, Toxicology & Endocrinology. Let’s take a look at the latest research on this compound (cas:2208-59-5).

The effects of eight newly synthesized 2-aryl substituted benzimidazole derivatives on control and phenobarbital (PB)-treated rat liver microsomal aniline 4-hydroxylase and ethylmorphine N-demethylase activities, and their binding to control and PB-treated rat liver microsomal oxidized cytochrome P 450 are presented. All compounds inhibited ethylmorphine N-demethylase activity with IC50 values ranging from 8.50 × 10-4 M to 27.83 × 10-4 M in control and from 2.80 × 10-4 M to 15.79 × 10-4 M in PB-treated rats. Aniline 4-hydroxylase activity was inhibited by all of the compounds tested having IC50 values in the range of 7.04 × 10-4 M to 31.37 × 10-4 M in PB-treated rats, but only five of the compounds showed inhibitory activity in control rats. Only a few significant regression coefficients could be found between the parameters of the chems. studied and their inhibitory patterns. No correlation has been observed between the binding of the derivatives and their inhibitory pattern. The compound 2-benzylbenzimidazole was prepared by refluxing o-phenylenediamine with phenylacetic acid.

This literature about this compound(2208-59-5)Related Products of 2208-59-5has given us a lot of inspiration, and I hope that the research on this compound(2-(Pyridin-4-yl)-1H-benzo[d]imidazole) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles